Rahmani Mohamed, Davis Eric Maynard, Bauer Cheryl, Dent Paul, Grant Steven
Departments of Medicine, Biochemistry, and Pharmacology, Virginia Commonwealth University, School of Medicine, Richmond, Virginia 23298.
J Biol Chem. 2005 Oct 21;280(42):35217-27. doi: 10.1074/jbc.M506551200. Epub 2005 Aug 18.
BAY 43-9006 is a kinase inhibitor that induces apoptosis in a variety of tumor cells. Here we report that treatment with BAY 43-9006 results in marked cytochrome c and AIF release into the cytosol, caspase-9, -8, -7, and -3 activation, and apoptosis in human leukemia cells (U937, Jurkat, and K562). Pronounced apoptosis was also observed in blasts from patients with acute myeloid leukemia. These events were accompanied by ERK1/2 inactivation and caspase-independent down-regulation of Mcl-1. Inducible expression of a constitutively active MEK1 construct did not prevent Mcl-1 down-regulation, suggesting that this event is not related to MEK/ERK pathway inactivation. Furthermore, BAY 43-9006 did not induce major changes in Mcl-1 mRNA levels monitored by real-time PCR or Mcl-1 promoter activity demonstrated by luciferase reporter assays, but it did enhance Mcl-1 down-regulation in actinomycin D-treated cells. Inhibition of protein synthesis by cycloheximide or proteasome function with MG132 and pulse-chase studies with [35S]methionine demonstrated that BAY 43-9006 did not diminish Mcl-1 protein stability, nor did it enhance Mcl-1 ubiquitination, but instead markedly attenuated Mcl-1 translation in association with the rapid and potent dephosphorylation of the eIF4E translation initiation factor. Finally, ectopic expression of Mcl-1 in leukemic cells markedly inhibited BAY 43-9006-mediated cytochrome c cytosolic release, caspase-9, -7, and -3 activation, as well as cell death, indicating that Mcl-1 operates upstream of cytochrome c release and caspase activation. Together, these findings demonstrate that BAY 43-9006 mediates cell death in human leukemia cells, at least in part, through down-regulation of Mcl-1 via inhibition of translation.
BAY 43-9006是一种激酶抑制剂,可诱导多种肿瘤细胞凋亡。在此我们报告,用BAY 43-9006处理会导致明显的细胞色素c和AIF释放到细胞质中,半胱天冬酶-9、-8、-7和-3激活,以及人白血病细胞(U937、Jurkat和K562)凋亡。在急性髓细胞白血病患者的原始细胞中也观察到明显的凋亡。这些事件伴随着ERK1/2失活和Mcl-1的非半胱天冬酶依赖性下调。组成型活性MEK1构建体的诱导性表达并不能阻止Mcl-1下调,这表明该事件与MEK/ERK途径失活无关。此外,BAY 43-9006并未引起实时PCR监测的Mcl-1 mRNA水平或荧光素酶报告基因检测显示的Mcl-1启动子活性的重大变化,但它确实增强了放线菌素D处理细胞中Mcl-1的下调。用环己酰亚胺抑制蛋白质合成或用MG132抑制蛋白酶体功能以及用[35S]甲硫氨酸进行脉冲追踪研究表明,BAY 43-9006既没有降低Mcl-1蛋白稳定性,也没有增强Mcl-1泛素化,而是与eIF4E翻译起始因子的快速有效去磷酸化相关联,显著减弱了Mcl-1翻译。最后,白血病细胞中Mcl-1的异位表达显著抑制了BAY 43-9006介导的细胞色素c细胞质释放、半胱天冬酶-9、-7和-3激活以及细胞死亡,表明Mcl-1在细胞色素c释放和半胱天冬酶激活的上游起作用。总之,这些发现表明BAY 43-9006至少部分地通过抑制翻译下调Mcl-1来介导人白血病细胞的死亡。